Associate Director, Clinical Operations

MSD


Job Location:

Petaling Jaya - Malaysia

Monthly Salary: Not Disclosed
Posted on: 6 hours ago
Vacancies: 1 Vacancy

Job Summary

Job Description

This role is accountable for the execution and oversight of local operational clinical trial activities in compliance with ICH/GCP and country regulations company policies and procedures and internal and external quality standards.

Under the oversight of the CRD or Head of Country Operations the position is responsible for managing and overseeing a team of Clinical Operations Managers (COMs) and/or Clinical Trial Coordinators (CTCs).

This role plays a critical role in delivering country-specific clinical trial commitments and objectives particularly during study start-up while ensuring operational excellence compliance quality and stakeholder alignment.

Key Responsibilities

Financial Management

  • Own country and site budgets.

  • Develop negotiate and complete Clinical Trial Research Agreements (CTRAs).

  • Partner with local clinical teams to deliver clinical and financial contracts within fair market value guidelines.

  • Oversee and track clinical research-related payments.

  • Manage payment reconciliation at study close-out.

  • Ensure compliance with FCPA requirements Denied Parties Screening and financial systems maintenance.

  • Support financial forecasting and operational budget tracking in conjunction with the CRD where applicable.

Regulatory Submissions & Local Documentation

  • Execute and oversee country-level clinical trial submissions and approvals for assigned protocols.

  • Develop local language materials including:

    • Informed Consent Forms (ICFs)

    • Study-related translations

    • Other required local documentation

  • Collaborate with IRBs/IECs and Regulatory Authorities on submission and approval activities.

Operational & Quality Oversight

  • Manage country deliverables timelines and protocol outcomes to meet local commitments.

  • Ensure quality and compliance standards are maintained across assigned protocols.

  • Contribute to the development and improvement of local and global SOPs.

  • Oversee contract workers including COMs CTCs and local vendors.

  • Manage direct reports through:

    • Performance management

    • Development planning

    • Coaching and mentoring

    • Issue resolution

Stakeholder Management & Collaboration

  • Work closely with internal and external stakeholders to ensure country deliverables are achieved.

Internal Stakeholders

  • Clinical Research Managers (CRMs)

  • Clinical Trial Coordinators (CTCs)

  • Clinical Research Associates (CRAs)

  • Clinical Operations Managers (COMs)

  • Clinical Quality Managers (CQMs)

  • Medical Affairs

  • Pharmacovigilance

  • Regulatory Affairs

  • Business Compliance

  • Finance

  • Legal

  • Global and regional functional teams

External Stakeholders

  • Investigators

  • Clinical trial sites

  • Vendors

  • Regulatory agencies

  • Ethics committees

  • Other external partners

Local Process Management

Provide oversight and coordination of:

  • Clinical and ancillary supplies management

  • Import and export requirements

  • Supply destruction processes

  • Local filing systems (electronic and hard copy)

  • Archiving and retention requirements

  • Insurance process management

Maintain and update country information within:

  • Clinical systems

  • Regulatory systems

  • Safety systems

  • Financial systems

Experience Required

  • Minimum 8 years of clinical research experience.

  • Minimum 2 years of people management or team oversight experience.

Core Competencies

Leadership & People Management

  • Demonstrated people management skills including managing teams across countries.

  • Ability to influence investigators vendors external partners and country stakeholders.

  • Proven ability to deliver commitments within timelines and budget with minimal supervision.

Clinical & Regulatory Expertise

  • Strong knowledge of:

    • Budget and contract negotiations

    • Local ethics and regulatory requirements

    • Submission and approval processes

    • Development of local informed consent documents

    • Study start-up and ongoing study deliverables

  • Extensive clinical project management experience.

  • Expertise in clinical regulatory and financial systems tools and metrics.

Risk Management & Decision Making

  • Ability to identify risks proactively and implement mitigation plans.

  • Strong problem-solving capabilities.

  • Independent decision-making skills with accountability for outcomes.

Communication & Interpersonal Skills

  • Excellent verbal and written communication skills.

  • Strong negotiation and influencing capabilities.

  • Effective coaching mentoring and training skills.

Organizational Effectiveness

  • Ability to manage multiple protocols and priorities simultaneously.

  • Strong planning coordination and organizational skills.

  • Ability to work effectively in global and virtual environments.

Language

  • Fluency in English and the local language.

Education Required

Bachelors Degree (or equivalent) in:

  • Business Finance

  • Business Administration

  • Life Sciences

  • Healthcare-related discipline

  • Equivalent relevant experience

Preferred

Masters Degree (or equivalent) in:

  • Business Finance

  • Business Administration

  • Life Sciences

  • Healthcare-related discipline

  • Equivalent relevant experience

Team Management Scope

  • Direct management of approximately 614 employees (COMs and/or CTCs).

  • Oversight of contractor COMs and CTCs where applicable.

Required Skills:

Adaptability Adaptability Budget Management Clinical Research Clinical Research Management Clinical Trial Documentation Clinical Trial Management Clinical Trial Planning Clinical Trials Clinical Trials Monitoring Clinical Trials Operations Cross-Cultural Awareness Decision Making Ethical Standards Financial Accounting Good Clinical Practice (GCP) Informed Consent Legal Archiving Medical Affairs Oncology Trials Organizational Performance Management People Leadership People Management Risk Evaluation And Mitigation Strategy (REMS) Risk Management 1 more

Preferred Skills:

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Employee Status:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

08/31/2026

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.


Required Experience:

Director

Job DescriptionThis role is accountable for the execution and oversight of local operational clinical trial activities in compliance with ICH/GCP and country regulations company policies and procedures and internal and external quality standards.Under the oversight of the CRD or Head of Country Oper...

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Merck & Co., Inc., Kenilworth, New Jersey, USA is known as “Merck” in the United States, Canada & Puerto Rico. We are known as “MSD” in Europe, Middle East, Africa, Latin America & Asia Pacific. We are a global biopharmaceutical leader with a diverse portfolio of prescription medicine ... View more

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